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(R)-2-methyl-2-[2'-(phenylmethoxy)ethyl]oxirane

Base Information Edit
  • Chemical Name:(R)-2-methyl-2-[2'-(phenylmethoxy)ethyl]oxirane
  • CAS No.:252651-57-3
  • Molecular Formula:C12H16O2
  • Molecular Weight:192.258
  • Hs Code.:
  • Mol file:252651-57-3.mol
(R)-2-methyl-2-[2'-(phenylmethoxy)ethyl]oxirane

Synonyms:(R)-2-methyl-2-[2'-(phenylmethoxy)ethyl]oxirane

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Chemical Property of (R)-2-methyl-2-[2'-(phenylmethoxy)ethyl]oxirane Edit
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Technology Process of (R)-2-methyl-2-[2'-(phenylmethoxy)ethyl]oxirane

There total 9 articles about (R)-2-methyl-2-[2'-(phenylmethoxy)ethyl]oxirane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at 20 ℃; for 1h;
DOI:10.1071/CH99091
Guidance literature:
With trimethylsilylazide; (R,R)-(salen)Cr(III); In isopropyl alcohol; at 20 ℃; for 6h;
DOI:10.1016/S0040-4039(99)01502-6
Guidance literature:
Multi-step reaction with 7 steps
1.1: 10.02 g / CH2Cl2; ethanol / 0.5 h
2.1: 84 percent / LiAlH4 / tetrahydrofuran / 18 h / Heating
3.1: 82 percent / p-toluenesulfonic acid / 24 h / 20 °C
4.1: NaH / tetrahydrofuran
4.2: 91 percent / tetrabutylammonium iodide / tetrahydrofuran / 24 h
5.1: 92 percent / aq. H2SO4 / tetrahydrofuran / 4 h / 40 °C
6.1: 91 percent / Et3N / CH2Cl2 / 0.17 h / -10 °C
7.1: 94 percent / 1,8-diazabicyclo[5.4.0]undec-7-ene / CH2Cl2 / 1 h / 20 °C
With lithium aluminium tetrahydride; sulfuric acid; sodium hydride; toluene-4-sulfonic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; In tetrahydrofuran; ethanol; dichloromethane; 1.1: Esterification / 2.1: Reduction / 3.1: cyclocondensation / 4.1: deprotonation / 4.2: benzylation / 5.1: Hydrolysis / 6.1: Esterification / 7.1: cyclocondensation;
DOI:10.1071/CH99091
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